HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795383Generated: November 3, 2026
3-Chloro-2,5-dimethylpyrazine → 2,5-Dimethyl-3-phenylpyrazine
https://huagongshe.com/reaction/1795383
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-2,5-dimethylpyrazine | HCID 66771 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,5-Dimethyl-3-phenylpyrazine | HCID 13642920 | 64.4% |
Reaction Steps
A solution of phenylmagnesium bromide (1M in THF, 5.6 mL, 5.6 mmol) is added to a solution of 3-chloro-2,5-dimethylpyrazine (346 mg, 2.42 mmol) and Fe(acac)3 (43 mg, 0.12 mmol) in THF (10 mL) at −30° C. After stirring for 30 min at that temperature, the reaction is quenched with brine, the aqueous layer is extracted with Et2O, the combined organic phases are dried over Na2SO4 and evaporated, and the residue is purified by flash chromatography (hexane/ethyl acetate, 10:1). After eluting a first fraction containing biphenyl (212 mg), one obtains 2,5-dimethyl-3-phenylpyrazine as a pale yellow syrup (287 mg, 64%). 1H NMR (300 MHz, CD2Cl2) δ 8.31 (s, 1H), 7.55–7.59 (m, 2H), 7.43–7.51 (m, 3H), 2.55 (s, 3H), 2.54 (s, 3H). 13C NMR (75 MHz, CD2Cl2) δ 152.7, 150.6, 148.4, 142.1, 139.5, 129.3, 128.7, 128.6, 22.7, 21.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026478B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-af417605eafc4f64b6c1d1a370bd2027 |
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| Source note | uspto-grants-2006_04 |
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